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01 1BENZYL ALCOHOL
02 1CEFIDEROCOL SULFATE TOSYLATE
03 1Cefiderocol
04 1Cefiderocol Sulfate Tosilate
05 2Cefiderocol Sulfate Tosylate
06 1Cefiderokolsulfattosilat
07 2DORIPENEM
08 3EDARAVONE
09 4Lusutrombopag
10 2Naldemedine
11 1Naldemedine Tosylate
12 2Naldemedine tosylate
13 1Naldemedintosylate
14 1Ospemifen
15 3Ospemifene
16 1SULFAMETHOXAZOLE
17 2SULFAMETHOXAZOLE; TRIMETHOPRIM
18 4TACRINE HYDROCHLORIDE
19 1TRAMADOL HYDROCHLORIDE
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01 10SHIONOGI
02 5SHIONOGI INC
03 11Shionogi B.V.
04 8Shionogi Bv
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01 4CAPSULE;ORAL
02 11Film Coated Tablet
03 3Film-Coated Tablet
04 2INJECTABLE;INTRAVENOUS
05 1LOTION;TOPICAL
06 1POWDER;INTRAVENOUS
07 1Powder For Concentrate For Infusion Solution
08 4Powder For Concentrate For Solution For Infusion
09 2SOLUTION;INTRAVENOUS
10 1SUSPENSION;ORAL
11 1TABLET, ORALLY DISINTEGRATING;ORAL
12 3TABLET;ORAL
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01 1105MG/5ML
02 11G
03 41g
04 1200MCG
05 5200mcg
06 1250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 130MG/100ML (0.3MG/ML)
08 13MG
09 23mg
10 1400MG;80MG
11 15% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
12 1500MG
13 1500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 150MG
15 160MG
16 160MG/100ML (0.6MG/ML)
17 360mg
18 1800MG;160MG
19 1EQ 10MG BASE
20 1EQ 1GM BASE/VIAL
21 1EQ 20MG BASE
22 1EQ 30MG BASE
23 1EQ 40MG BASE
24 1Blank
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01 4Denmark
02 4Estonia
03 3Norway
04 4Spain
05 4Sweden
06 15USA
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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : LOTION;TOPICAL
Brand Name : ULESFIA
Dosage Strength : 5% **Federal Register ...
Packaging :
Approval Date : 2009-04-09
Application Number : 22129
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : Prescription
Registration Country : Estonia
Dosage Form : Powder For Concentrate F...
Brand Name : Fetcroja
Dosage Strength : 1g
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Powder For Concentrate F...
Brand Name : Fetcroja
Dosage Strength : 1g
Packaging :
Approval Date : 23-04-2020
Application Number : 28106239419
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : FETROJA
Dosage Strength : EQ 1GM BASE/VIAL
Packaging :
Approval Date : 2019-11-14
Application Number : 209445
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Powder For Concentrate F...
Brand Name : Fetcroja
Dosage Strength : 1G
Packaging :
Approval Date : 02-06-2020
Application Number : 1201434
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Powder For Concentrate F...
Brand Name : Fatcroja
Dosage Strength : 1g
Packaging :
Approval Date : 23-04-2020
Application Number : 2.02E+13
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Powder For Concentrate F...
Brand Name : Fetcroja
Dosage Strength : 1g
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : DORIBAX
Dosage Strength : 500MG/VIAL **Federal R...
Packaging :
Approval Date : 2007-10-12
Application Number : 22106
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INTRAVENOUS
Brand Name : DORIBAX
Dosage Strength : 250MG/VIAL **Federal R...
Packaging :
Approval Date : 2010-10-05
Application Number : 22106
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : RADICAVA
Dosage Strength : 30MG/100ML (0.3MG/ML)
Packaging :
Approval Date : 2017-05-05
Application Number : 209176
Regulatory Info : DISCN
Registration Country : USA

Shionogi is a supplier offers 19 products (APIs, Excipients or Intermediates).
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